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Journal of Cell Science|July 29, 2018
Functional analyses of Pericentrin and Syne-2 interaction in ciliogenesisNathalie Falk, Kristin Kessler, Sinja-Fee Schramm, et al.American Journal of Human Genetics|October 28, 2005
Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulatorChristian T Thiel, Denise Horn, Bernhard Zabel, et al.Human Mutation|October 18, 2014
MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulationDiana Zahnleiter, Nadine N Hauer, Kristin Kessler, et al.International Journal of Cancer|August 22, 2014
Comprehensive screening for mutations associated with colorectal cancer in unselected cases reveals penetrant and nonpenetrant mutationsCornelia Kraus, Tilman T Rau, Philipp Lux, et al.Molecular Syndromology|October 30, 2010
Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial DiverticulumA B Ekici, D Hilfinger, M Jatzwauk, et al.American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychiaC Bergmann, J Senderek, D Anhuf, et al.Frontiers in Oncology|November 7, 2025
An analysis of the distribution of bone and soft tissue sarcoma diagnoses and their disparities in Southwest Germany: a multicenter approachBranko Calukovic, Katrin Benzler, Mary E Carter, et al.Frontiers in Oncology|November 24, 2025
Correction: An analysis of the distribution of bone and soft tissue sarcoma diagnoses and their disparities in Southwest Germany: a multicenter approachBranko Calukovic, Katrin Benzler, Mary E Carter, et al.Journal of Medical Genetics|June 16, 2009
Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1U Hüffmeier, J Lascorz, T Becker, et al.Scientific Reports|July 2, 2015
DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defectsKristin Kessler, Ina Wunderlich, Steffen Uebe, et al.Pageof 14